Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010757606

FEI Number

3010757606

Entity Name

AbbVie Inc

City/State/Country

North Chicago, IL, US

Establishment Address

1 N Waukegan Rd, North Chicago, IL 60064, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

AbbVie Inc. (Owner Number: 10046068)

Owner / Operator Contact Address

1 N. Waukegan Rd, J23, North Chicago, IL 60064, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

AbbVie PEG AbbVie NJ AbbVie J AbbVie Cross Body Pack AbbVie Chest Pack AbbVie Snug Vest Abbvie Lightweight Vest AbbVie Hip Pack AbbVie Fitted Belt AbbVie Fitted Vest AbbVie Combined Fitted Vest AbbVie Belt Pouch for Vyafuser

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KNT	Tubes, Gastrointestinal (And Accessories)	Gastroenterology, Urology	Class 2	876.5980	2015-01-21
KNT	Tubes, Gastrointestinal (And Accessories)	Gastroenterology, Urology	Class 2	876.5980	2015-02-04
KNT	Tubes, Gastrointestinal (And Accessories)	Gastroenterology, Urology	Class 2	876.5980	2015-01-21
IQG	Adaptor, Holder, Syringe	Physical Medicine	Class 1	890.5050	2016-06-15

Official Correspondent

Michael McCoy

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AbbVie Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3002807401	AbbVie Deutschland GmbH & Co.KG	Ludwigshafen Rhineland-Palatinate, DE
3011299837	AbbVie US LLC	North Chicago, IL, US
3012441529	AbbVie Ireland NL B.V. Ballytivnan	Sligo, IE

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K900590	Biosearch Medical Products, Inc.	BIOSEARCH DOBBHOFF(R) GASTROTRAC JEJUNAL FEEDING	1990-08-02
K102548	Footprint Medical, Inc.	FOOTPRINT MEDICAL POLYURETHANE FEEDING TUBE	2010-11-26
K955248	United States Endoscopy Group, Inc.	U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT	1996-05-21
K872921	Medical Support, Inc.	MSS ENTERAL DELIVERY SET	1987-12-03
K180622	Covidien	Kangaroo Gastrostomy Feeding Tube with ENFit Y-Port	2018-10-23

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3015237508	ADVANCED MEDICAL BALLOONS GMBH	Waghaeusel Baden-Wurttemberg, DE
3009247326	Jabil Circuit (Singapore) Pte Ltd	Singapore Central Singapore, SG
2528981	LYNX Medical Pennsylvania	ERIE, PA, US
1649518	Sterigenics US LLC	Fort Worth, TX, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010757606. Last updated year: 2026. Please use registration number 3010757606 when referencing this establishment in official correspondence.